LeMaitre Vascular, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1757-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

AlboGraft Knitted with Collagen, Bifurcate 18x09 Catalog Number: AMC1809 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.

Product Classification:

Class I

Date Initiated: June 17, 2013

Date Posted: July 31, 2013

Recall Number: Z-1757-2013

Event ID: 65553

Reason for Recall:

Blood blushing/leaking from the surface of the graft after implantation

Status: Terminated

Product Quantity: 3 units

Code Information:

Lot number/Expiration Date 56890A 2015-04

Distribution Pattern:

Worldwide distribution: USA including PA and countries of: BRAZIL, BULGARIA, FRANCE, GEORGIA, GERMANY, GREECE, ITALY, LEBANON, NETHERLAND, POLAND, SPAIN, and TURKEY.

Voluntary or Mandated:

Voluntary: Firm initiated